Tissue expression of the novel serine carboxypeptidase Scpep1

Ting Hein D. Lee, Jeffrey W. Streb, Mary A. Georger, Joseph M. Miano

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


We previously identified a novel gene designated retinoid-inducible serine carboxypeptidase (RISC or Scpep1). Here we characterize a polyclonal antibody raised to Scpep1 and assess its localization in mouse cells and tissues. Western blot analysis revealed an immunospecific ∼35-kDa protein corresponding to endogenous Scpep1. This protein is smaller than the predicted ∼51-kDa, suggesting that Scpep1 is proteolytically cleaved to a mature enzyme. Immunohistochemical studies demonstrate Scpep1 expression in embryonic heart and vasculature as well as in adult aortic smooth muscle cells and endothelial cells. Scpep1 displays a broad expression pattern in adult tissues with detectable levels in epithelia of digestive tract and urinary bladder, islet of Langerhans, type II alveolar cells and macrophages of lung, macrophage-like cells of lymph nodes and spleen, Leydig cells of testis, and nerve fibers in brain and ganglia. Consistent with previous mRNA studies in kidney, Scpep1 protein is restricted to proximal convoluted tubular epithelium (PCT). Immunoelectron microscopy shows enriched Scpep1 within lysosomes of the PCT, and immunofluorescence microscopy colocalizes Scpep1 with lysosomal-associated membrane protein-2. These results suggest that Scpep1 is a widely distributed lysosomal protease requiring proteolytic cleavage for activity. The highly specific Scpep1 antibody characterized herein provides a necessary reagent for elucidating Scpep1 function.

Original languageEnglish (US)
Pages (from-to)701-711
Number of pages11
JournalJournal of Histochemistry and Cytochemistry
Issue number6
StatePublished - Jun 2006
Externally publishedYes


  • Immunolocalization
  • Immunospecificity
  • Lysosomal-associated membrane protein-2
  • Lysosome
  • Retinoid-inducible serine carboyxpeptidase
  • Serine carboxypeptidase

ASJC Scopus subject areas

  • Anatomy
  • Histology


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